Chevallier P, Labopin M, Milpied N, Bilger K, Socié G, Yakoub-Agha I, Michallet M, Bulabois C-E, Maury S, Beguin Y, Bay J-O, Blaise D, Maillard N, Guillerm G, Daguindeau E, Raus N, Mohty M
Centre Hospitalier et Universitaire (CHU) de Nantes, Hématologie Clinique, Centre d'Investigation Clinique en Cancérologie (CI2C), Université de Nantes and INSERM CRNCA UMR 892, Nantes, France.
1] Hématologie Clinique et Thérapie Cellulaire, Hopital Saint-Antoine, APHP, Paris, France [2] EBMT, ALWP Office, Hopital Saint Antoine, Paris, France [3] Universite Pierre et Marie Curie (UPMC), Paris, France [4] INSERM UMRs 938, Paris, France.
Bone Marrow Transplant. 2014 Mar;49(3):361-5. doi: 10.1038/bmt.2013.186. Epub 2013 Dec 2.
Previous data suggested that allo-SCT might be an effective therapy in the setting of chemo-refractory/relapsed diseases because of the potent long-term immune-mediated tumor control. This retrospective study aimed to analyze the outcome of adult patients who received allo-SCT in a chemo-refractory/relapsed status. The series included 840 patients with active or progressive disease at the time of transplant. Median age was 50 years. With a median follow-up of 40 months, 3-year OS, disease-free survival (DFS), and non-relapse mortality rates were 29±2, 23±2, and 30±2%, respectively. At the last follow-up, 252 patients (30%) were still alive (of whom 201 were in CR (24%). In a Cox multivariate analysis, the use of a reduced-intensity conditioning (RIC) before allo-SCT and use of an HLA-identical sibling donor remained independently associated with a better OS (hazard ratio (HR)=0.82; 95% confidence interval (CI), 0.69-0.98, P=0.03; and HR=0.79; 95% CI, 0.66-0.93, P=0.006, respectively). Also, a diagnosis of myelodysplastic syndrome/myeloproliferative disorder, Hodgkin lymphoma and non-Hodgkin lymphoma compared with acute leukemia had a favorable impact on OS (HR=0.55; 95% CI, 0.45-0.68, P<0.0001; HR=0.49; 95% CI, 0.31-0.75, P=0.001; and HR=0.47; 95% CI, 0.35-0.63, P<0.0001, respectively). In conclusion, this study suggests that allo-SCT may be of benefit in some subgroups of patients with active or progressive hematological malignancies at the time of allo-SCT.
既往数据表明,由于具有强大的长期免疫介导的肿瘤控制作用,异基因造血干细胞移植(allo-SCT)可能是化疗难治性/复发性疾病的一种有效治疗方法。这项回顾性研究旨在分析处于化疗难治性/复发状态时接受allo-SCT的成年患者的预后。该系列研究纳入了840例移植时患有活动性或进展性疾病的患者。中位年龄为50岁。中位随访40个月,3年总生存期(OS)、无病生存期(DFS)和非复发死亡率分别为29±2%、23±2%和30±2%。在最后一次随访时,252例患者(30%)仍存活(其中201例处于完全缓解(CR)状态(24%))。在Cox多因素分析中,allo-SCT前采用减低强度预处理(RIC)以及使用人类白细胞抗原(HLA)相合同胞供者仍分别独立与更好的OS相关(风险比(HR)=0.82;95%置信区间(CI),0.69 - 0.98,P = 0.03;以及HR = 0.79;95% CI,0.66 - 0.93,P = 0.006)。此外,与急性白血病相比,骨髓增生异常综合征/骨髓增殖性疾病、霍奇金淋巴瘤和非霍奇金淋巴瘤的诊断对OS有有利影响(HR分别为0.55;95% CI,0.45 - 0.68,P < 0.0001;HR = 0.49;95% CI,0.31 - 0.75,P = 0.001;以及HR = 0.47;95% CI,0.35 - 0.63,P < 0.0001)。总之,本研究提示allo-SCT可能对allo-SCT时患有活动性或进展性血液系统恶性肿瘤的部分亚组患者有益。